Interactions of bacterial cationic peptide antibiotics with outer and cytoplasmic membranes of Pseudomonas aeruginosa. Antimicrob. Agents Chemother

Polymyxins B and E1 and gramicidin S are bacterium-derived cationic antimicrobial peptides. The poly-myxins were more potent than gramicidin S against Pseudomonas aeruginosa, with MICs of 0.125 to 0.25 and 8 mg/ml, respectively. These peptides differed in their affinities for binding to lipopolysaccharide, but all were able to permeabilize the outer membrane of wild-type P. aeruginosa PAO1 strain H103, suggesting differences in their mechanisms of self-promoted uptake. Gramicidin S caused rapid depolarization of the bacterial cytoplasmic membrane at concentrations at which no killing was observed within 30 min, whereas, conversely, the concentrations of the polymyxins that resulted in rapid killing resulted in minimal depolarization. These data indicate that the depolarization of the cytoplasmic membrane by these peptides did not correlate with bacterial cell lethality. Gramicidin S and the polymyxins are nonribosomally pro-duced peptides obtained from bacteria. They have achieved widespread usage as topical agents (4). Gramicidin S is a di-basic cyclic decapeptide with a two-stranded antiparallel b-sheet structure with the strands interconnected by two type II b-turns (4, 6). The polymyxins, including polymyxin B an